Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring von Bessa, Paraskevi, Newman, Andrew G., Yan, Kuo, Schaub, Theres, Dannenberg, Rike, Lajkó, Denis, Eilenberger, Julia, Brunet, Theresa, Textoris-Taube, Kathrin, Kemmler, Emanuel, Deng, Penghui, Banerjee, Priyanka, Ravindran, Ethiraj, Preissner, Robert, Rosário, Marta, Tarabykin, Victor

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Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly von Ravindran, Ethiraj, Lesca, Gaetan, Januel, Louis, Goldgruber, Linus, Dickmanns, Achim, Margot, Henri, Kaindl, Angela M

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Monoallelic CRMP1 gene variants cause neurodevelopmental disorder von Ravindran, Ethiraj, Arashiki, Nobuto, Becker, Lena-Luise, Takizawa, Kohtaro, Lévy, Jonathan, Rambaud, Thomas, Makridis, Konstantin L, Goshima, Yoshio, Li, Na, Vreeburg, Maaike, Demeer, Bénédicte, Dickmanns, Achim, Stegmann, Alexander P A, Hu, Hao, Nakamura, Fumio, Kaindl, Angela M

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Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease von Ravindran, Ethiraj, Ullah, Noor, Mani, Shyamala, Chew, Elaine Guo Yan, Tandiono, Moses, Foo, Jia Nee, Khor, Chiea Chuen, Kaindl, Angela M., Siddiqi, Saima

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Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation von Ravindran, Ethiraj, Hu, Hao, Yuzwa, Scott A, Hernandez-Miranda, Luis R, Kraemer, Nadine, Ninnemann, Olaf, Musante, Luciana, Boltshauser, Eugen, Schindler, Detlev, Hübner, Angela, Reinecker, Hans-Christian, Ropers, Hans-Hilger, Birchmeier, Carmen, Miller, Freda D, Wienker, Thomas F, Hübner, Christoph, Kaindl, Angela M

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Novel Alternative Splice Variants of Mouse Cdk5rap2 von Kraemer, Nadine, Issa-Jahns, Lina, Neubert, Gerda, Ravindran, Ethiraj, Mani, Shyamala, Ninnemann, Olaf, Kaindl, Angela M

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Arhgef2 regulates neural differentiation in the cerebral cortex through mRNA m6A-methylation of Npdc1 and Cend1 von Zhou, Pei, Qi, Yifei, Fang, Xiang, Yang, Miaomiao, Zheng, Shuxin, Liao, Caihua, Qin, Fengying, Liu, Lili, Li, Hong, Li, Yan, Ravindran, Ethiraj, Sun, Chuanbo, Wei, Xinshu, Wang, Wen, Fang, Liang, Han, Dingding, Peng, Changgeng, Chen, Wei, Li, Na, Kaindl, Angela M., Hu, Hao

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Differential expression of Brn3 transcription factors in intrinsically photosensitive retinal ganglion cells in mouse von Jain, Varsha, Ravindran, Ethiraj, Dhingra, Narender K.

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PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients von Picker-Minh, Sylvie, Luperi, Ilaria, Ravindran, Ethiraj, Kraemer, Nadine, Zaqout, Sami, Stoltenburg-Didinger, Gisela, Ninnemann, Olaf, Hernandez-Miranda, Luis R., Mani, Shyamala, Kaindl, Angela M.

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Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders von Ravindran, Ethiraj, Jühlen, Ramona, Vieira-Vieira, Carlos H, Ha, Thuong, Salzberg, Yuval, Fichtman, Boris, Luise-Becker, Lena, Martins, Nuno, Picker-Minh, Sylvie, Bessa, Paraskevi, Arts, Peer, Jackson, Matilda R, Taranath, Ajay, Kamien, Benjamin, Barnett, Christopher, Li, Na, Tarabykin, Victor, Stoltenburg-Didinger, Gisela, Harel, Amnon, Selbach, Matthias, Dickmanns, Achim, Fahrenkrog, Birthe, Hu, Hao, Scott, Hamish, Kaindl, Angela M

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Proteome changes in autosomal recessive primary microcephaly von Zaqout, Sami, Mannaa, Atef, Klein, Oliver, Krajewski, Angelika, Klose, Joachim, Luise‐Becker, Lena, Elsabagh, Ahmed, Ferih, Khaled, Kraemer, Nadine, Ravindran, Ethiraj, Makridis, Konstantin, Kaindl, Angela M.

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Congenital microcephaly‐linked CDK5RAP2 affects eye development von Zaqout, Sami, Ravindran, Ethiraj, Stoltenburg‐Didinger, Gisela, Kaindl, Angela M.

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Identification and characterization of mechanisms underlying intellectual disability von Ravindran, Ethiraj

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Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2) von von Bernuth, Horst, Ravindran, Ethiraj, Du, Hang, Fröhler, Sebastian, Strehl, Karoline, Krämer, Nadine, Issa-Jahns, Lina, Amulic, Borko, Ninnemann, Olaf, Xiao, Mei-Sheng, Eirich, Katharina, Kölsch, Uwe, Hauptmann, Kathrin, John, Rainer, Schindler, Detlev, Wahn, Volker, Chen, Wei, Kaindl, Angela M

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Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation von Farag, Heba Gamal, Froehler, Sebastian, Oexle, Konrad, Ravindran, Ethiraj, Schindler, Detlev, Staab, Timo, Huebner, Angela, Kraemer, Nadine, Chen, Wei, Kaindl, Angela M

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Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes von Kraemer, Nadine, Ravindran, Ethiraj, Zaqout, Sami, Neubert, Gerda, Schindler, Detlev, Ninnemann, Olaf, Gräf, Ralph, Seiler, Andrea E M, Kaindl, Angela M

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Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation von Ravindran, Ethiraj, Hu, Hao, Yuzwa, Scott A, Hernandez-Miranda, Luis R, Kraemer, Nadine, Ninnemann, Olaf, Musante, Luciana, Boltshauser, Eugen, Schindler, Detlev, Hübner, Angela, Reinecker, Hans-Christian, Ropers, Hans-Hilger, Birchmeier, Carmen, Miller, Freda D, Wienker, Thomas F, Hübner, Christoph, Kaindl, Angela M

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Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly von Ravindran, Ethiraj, Lesca, Gaetan, Januel, Louis, Goldgruber, Linus, Dickmanns, Achim, Margot, Henri, Kaindl, Angela M

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Congenital microcephaly‐linked CDK5RAP2 affects eye development von Zaqout, Sami, Ravindran, Ethiraj, Stoltenburg‐Didinger, Gisela, Kaindl, Angela M

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Proteome changes in autosomal recessive primary microcephaly von Zaqout, Sami, Mannaa, Atef, Klein, Oliver, Krajewski, Angelika, Klose, Joachim, Luise‐Becker, Lena, Elsabagh, Ahmed, Ferih, Khaled, Kraemer, Nadine, Ravindran, Ethiraj, Makridis, Konstantin, Kaindl, Angela M

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